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FDA 510(k)

DIA ANATOMIC ABUTMENT

K-Number: K902433 · 1992-01-17

ApplicantDental Imaging Assoc., Inc.
Decision Date1992-01-17
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DIA ANATOMIC ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Dental Imaging Assoc., Inc.. It received FDA 510(k) clearance on 1992-01-17 under 510(k) number K902433. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIA ANATOMIC ABUTMENT?

DIA ANATOMIC ABUTMENT is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Dental Imaging Assoc., Inc.. The 510(k) number is K902433.

When did DIA ANATOMIC ABUTMENT receive FDA 510(k) clearance?

DIA ANATOMIC ABUTMENT received FDA 510(k) clearance on 1992-01-17, under 510(k) number K902433.

Who is the listed applicant for DIA ANATOMIC ABUTMENT?

The FDA 510(k) record lists Dental Imaging Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIA ANATOMIC ABUTMENT?

The FDA product code for DIA ANATOMIC ABUTMENT is DZE.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Dental Imaging Assoc., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K902434DIA HEALING CAPK902435DIA IMPRESSION COPING

Related Devices (Code: DZE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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